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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7015152copy number variation1nstd229human GRCh38 chr19: 35,612,506-35,614,330 , GRCh37.p13 chr19: 36,103,408-36,105,232 HAUS5
    nsv7013640copy number variation1nstd229human GRCh38 chr19: 35,616,301-35,619,600 , GRCh37.p13 chr19: 36,107,203-36,110,502 HAUS5, TRUND-NNN10-1
    nsv7011118copy number variation1nstd229human GRCh38 chr19: 35,602,828-35,635,989 , GRCh37.p13 chr19: 36,093,730-36,126,891 HAUS5, RBM42, 1 more genes
    nsv7009658copy number variation1nstd229human GRCh38 chr19: 35,623,993-35,627,965 , GRCh37.p13 chr19: 36,114,895-36,118,867 RBM42, HAUS5
    nsv7008200copy number variation1nstd229human GRCh38 chr19: 35,500,961-35,647,974 , GRCh37.p13 chr19: 35,991,863-36,138,876 SBSN, TMEM147-AS1, 10 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7000608copy number variation1nstd229human GRCh38 chr19: 35,610,097-35,612,700 , GRCh37.p13 chr19: 36,100,999-36,103,602 HAUS5
    nsv6525602copy number variation1nstd223human GRCh38 chr19: 35,623,993-35,627,961 , GRCh37.p13 chr19: 36,114,895-36,118,863 RBM42, HAUS5
    nsv6518836copy number variation1nstd223human GRCh38 chr19: 35,616,394-35,619,635 , GRCh37.p13 chr19: 36,107,296-36,110,537 HAUS5, TRUND-NNN10-1
    nsv6310629copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407 KRTDAP, WDR62, 78 more genes
    nsv6291710copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,019,064-36,516,110 , GRCh38.p12 chr19: 35,528,162-36,025,208 NFKBID, APLP1, 38 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5027700copy number variation1nstd200human GRCh38 chr19: 35,616,394-35,619,635 , GRCh37.p13 chr19: 36,107,296-36,110,537 TRUND-NNN10-1, HAUS5
    nsv5024567copy number variation1nstd200human GRCh38 chr19: 35,625,233-35,625,387 , GRCh37.p13 chr19: 36,116,135-36,116,289 HAUS5
    nsv4727920copy number variation1nstd197human GRCh38.p12 chr19: 35,618,403-35,619,049 , GRCh37 chr19: 36,109,305-36,109,951 HAUS5, TRUND-NNN10-1
    nsv4674329copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397 LOC105372379, LSR, 50 more genes
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